rs11276
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs11276(A;A) |
| Make rs11276(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 12 |
| Position | 14840505 |
| Gene | ART4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11276 |
| dbSNP (classic) | rs11276 |
| ClinGen | rs11276 |
| ebi | rs11276 |
| HLI | rs11276 |
| Exac | rs11276 |
| Gnomad | rs11276 |
| Varsome | rs11276 |
| LitVar | rs11276 |
| Map | rs11276 |
| PheGenI | rs11276 |
| Biobank | rs11276 |
| 1000 genomes | rs11276 |
| hgdp | rs11276 |
| ensembl | rs11276 |
| geneview | rs11276 |
| scholar | rs11276 |
| rs11276 | |
| pharmgkb | rs11276 |
| gwascentral | rs11276 |
| openSNP | rs11276 |
| 23andMe | rs11276 |
| SNPshot | rs11276 |
| SNPdbe | rs11276 |
| MSV3d | rs11276 |
| GWAS Ctlg | rs11276 |
| GMAF | 0.2801 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | rs11276(A;A) |
| Alt | rs11276(A;A) |
| Reference | Rs11276(G;G) |
| Significance | Other |
| Disease | Blood group |
| Variation | info |
| Gene | ART4 |
| CLNDBN | Blood group, Dombrock system |
| Reversed | 1 |
| HGVS | NC_000012.11:g.14993439C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000019304.29, |
[PMID 21257350
] DNA-based methods in the immunohematology reference laboratory.
{{on chip | Illumina Human 1M}
This SNP is associated with the Dombrock blood group [PMID 11001920]
